Interactions in the network of Usher syndrome type 1 proteins-Reference-Cited by-同舟云学术

Interactions in the network of Usher syndrome type 1 proteins

Published:2004-12-08 Issue:3 Volume:14 Page:347-356
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Adato Avital,Michel Vincent,Kikkawa Yoshiaki,Reiners Jan,Alagramam Kumar N.,Weil Dominique,Yonekawa Hiromichi,Wolfrum Uwe,El-Amraoui Aziz,Petit Christine

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/14/3/347/2235123/ddi031.pdf

Reference44 articles.

1. Petit, C. (2001) Usher syndrome: from genetics to pathogenesis. Annu. Rev. Genom. Hum. Genet., 2, 271–297.

2. Weil, D., Blanchard, S., Kaplan, J., Guilford, P., Gibson, F., Walsh, J., Mburu, P., Varela, A., Levilliers, J., Weston, M.D. et al. (1995) Defective myosin VIIA gene responsible for Usher syndrome type 1B. Nature, 374, 60–61.

3. Bitner-Glindzicz, M., Lindley, K.J., Rutland, P., Blaydon, D., Smith, V.V., Milla, P.J., Hussain, K., Furth-Lavi, J., Cosgrove, K.E., Shepherd, R.M. et al. (2000) A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene. Nat. Genet., 26, 56–60.

4. Verpy, E., Leibovici, M., Zwaenepoel, I., Liu, X.-Z., Gal, A., Salem, N., Mansour, A., Blanchard, S., Kobayashi, I., Keats, B.J.B. et al. (2000) A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C. Nat. Genet., 26, 51–55.

5. Bolz, H., von Brederlow, B., Ramirez, A., Bryda, E.C., Kutsche, K., Nothwang, H.G., Seeliger, M., Salcedo Cabrera, M.d.C., Vila, M.C., Molina, O.P. et al. (2001) Mutations of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D. Nat. Genet., 27, 108–112.

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